Mediteam AB
SwedenFDA applicant, unverified
- Devices
- 1
What Mediteam AB makes
Mediteam AB manufactures mechanical power drives designed for medical applications, including those used in surgical and diagnostic equipment. These devices are engineered to provide controlled motion for procedures requiring precise actuation, such as robotic-assisted systems or adjustable patient positioning.
The company’s portfolio is regulated under Class I medical devices in the US, with relevant products listed via the FDA’s 510(k) pathway. The manufacturer operates from the United States, adhering to applicable regulatory standards for device clearance and compliance.
Catalogue
Power Drive Ref K012944
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mediteam AB have in the registry?
The registry currently lists 1 device for Mediteam AB. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mediteam AB's devices?
Among its 1 most recently registered device, Mediteam AB has devices listed in FDA 510(k) (1 device).
What risk classes do Mediteam AB's devices fall under?
Among its 1 most recently registered device, the classes recorded for Mediteam AB's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Mediteam AB in the registry?
The most recently registered devices listed for Mediteam AB include POWER DRIVE.